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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 600622Generated: October 30, 2026

2-Amino-5-nitropyridine → HCID 67273481, compound

https://huagongshe.com/reaction/600622

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-5-nitropyridineHCID 77888—
Reactant3-Bromo-1-phenylpropane-1,2-dioneHCID 12568911—
SolventEthanolHCID 702—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67273481HCID 6727348187.5%

Reaction Conditions

Temperature160 °C

Reaction Steps

To a solution of 0.48 g of 3-bromo-1-phenylpropane-1,2-dione in a mixture of 3 mL of THF and 0.5 mL of ethanol is added 0.25 g of 2-amino-5-nitropyridine. The reaction mixture is heated for 15 minutes at 160° C. in a microwave machine. The solid formed is separated out, taken up in 3 mL of ethanol and refluxed for 6 hours. After evaporating off the solvent, the residue is taken up in ethyl acetate and diluted with sodium hydroxide solution. The organic phase is washed with water, dried and then evaporated to give 0.42 g of (6-nitroimidazo[1,2-a]pyridin-2-yl)(phenyl)methanone in the form of a brown solid, which is used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07902219B2
Source datasetuspto-grants-2011_03
ORD IDord-f68d61f29edf4a5db764361f4214abe6
Source noteuspto-grants-2011_03